rs11119328
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs11119328(A;A) |
| Make rs11119328(A;C) |
| Make rs11119328(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 209711973 |
| Gene | HSD11B1, LOC101930114 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11119328 |
| dbSNP (classic) | rs11119328 |
| ClinGen | rs11119328 |
| ebi | rs11119328 |
| HLI | rs11119328 |
| Exac | rs11119328 |
| Gnomad | rs11119328 |
| Varsome | rs11119328 |
| LitVar | rs11119328 |
| Map | rs11119328 |
| PheGenI | rs11119328 |
| Biobank | rs11119328 |
| 1000 genomes | rs11119328 |
| hgdp | rs11119328 |
| ensembl | rs11119328 |
| geneview | rs11119328 |
| scholar | rs11119328 |
| rs11119328 | |
| pharmgkb | rs11119328 |
| gwascentral | rs11119328 |
| openSNP | rs11119328 |
| 23andMe | rs11119328 |
| SNPshot | rs11119328 |
| SNPdbe | rs11119328 |
| MSV3d | rs11119328 |
| GWAS Ctlg | rs11119328 |
| GMAF | 0.1873 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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[PMID 22112815] The Effect of Common Genetic Variation in 11?-Hydroxysteroid Dehydrogenase Type 1 on Hypothalamic-Pituitary-Adrenal Axis Activity and Incident Depression
[PMID 24915124] Common genetic variants in the glucocorticoid receptor and the 11β-Hydroxysteroid dehydrogenase type 1 genes influence long-term cognitive impairments in patients with Cushing's syndrome in remission
